Guest guest Posted January 14, 2008 Report Share Posted January 14, 2008 Hi Deon, We welcome you to our group. We do however hate the reason you needed to find us. You will get your questions answered by people who have suffered with this disease (the monster) for all different periods of time. This is a wonderful group.Are you on oxygen yet? That is probably what is going on. Love and Prayers, Peggy ipf 6/04 Florida"Worry looks around, Sorry looks back, Faith looks up." Hello everyone,I'm new to the group, but was very excited to know that such a support group existed. I'm a 37 yr old wife and mother of a 16 and 12 yr old. I was diagnosed with Mixed connective tissue disease three years ago, and pulmonary fibrosis in 2006. At this time, the fibrosis has been difficult, when I laugh I cough, when I talk too long I get winded, and as you all know, simple things like showering and curling my hair is a task. Boy what I would give to feel normal again. Deon, Lithonia, GaNever miss a thing. Make Yahoo your homepage. Quote Link to comment Share on other sites More sharing options...
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